Clarimon J - Search Results

1

Analysis of SCA-2 and SCA-3 repeats in Parkinsonism: evidence of SCA-2 expansion in a family with autosomal dominant Parkinson's disease.

Simon-Sanchez J, Hanson M, Singleton A, Hernandez D, McInerney A, Nussbaum R, Werner J, Gallardo M, Weiser R, Gwinn-Hardy K, Singleton AB, Clarimon J. Simon-Sanchez J, et al. Among authors: clarimon j. Neurosci Lett. 2005 Jul 1-8;382(1-2):191-4. doi: 10.1016/j.neulet.2005.03.015. Epub 2005 Apr 1. Neurosci Lett. 2005. PMID: 15911147

2

Alpha-synuclein in blood and brain from familial Parkinson disease with SNCA locus triplication.

Miller DW, Hague SM, Clarimon J, Baptista M, Gwinn-Hardy K, Cookson MR, Singleton AB. Miller DW, et al. Among authors: clarimon j. Neurology. 2004 May 25;62(10):1835-8. doi: 10.1212/01.wnl.0000127517.33208.f4. Neurology. 2004. PMID: 15159488

3

Paraoxonase 1 (PON1) gene polymorphisms and Parkinson's disease in a Finnish population.

Clarimon J, Eerola J, Hellström O, Tienari PJ, Singleton A. Clarimon J, et al. Neurosci Lett. 2004 Sep 2;367(2):168-70. doi: 10.1016/j.neulet.2004.05.108. Neurosci Lett. 2004. PMID: 15331145

4

Defining the ends of Parkin exon 4 deletions in two different families with Parkinson's disease.

Clarimon J, Johnson J, Dogu O, Horta W, Khan N, Lees AJ, Hardy J, Singleton A. Clarimon J, et al. Am J Med Genet B Neuropsychiatr Genet. 2005 Feb 5;133B(1):120-3. doi: 10.1002/ajmg.b.30119. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 15635662

5

Mutation of the Parkin gene in a Persian family: clinical progression over a 40-year period.

Clarimon J, Johnson J, Djaldetti R, Hernandez D, Hattori N, Sroka H, Barhom Y, Singleton A. Clarimon J, et al. Mov Disord. 2005 Jul;20(7):887-90. doi: 10.1002/mds.20495. Mov Disord. 2005. PMID: 15852366

6

Torsin A haplotype predisposes to idiopathic dystonia.

Clarimon J, Asgeirsson H, Singleton A, Jakobsson F, Hjaltason H, Hardy J, Sveinbjornsdottir S. Clarimon J, et al. Ann Neurol. 2005 May;57(5):765-7. doi: 10.1002/ana.20485. Ann Neurol. 2005. PMID: 15852391

7

Lack of evidence for a genetic association between FGF20 and Parkinson's disease in Finnish and Greek patients.

Clarimon J, Xiromerisiou G, Eerola J, Gourbali V, Hellström O, Dardiotis E, Peuralinna T, Papadimitriou A, Hadjigeorgiou GM, Tienari PJ, Singleton AB. Clarimon J, et al. BMC Neurol. 2005 Jun 20;5:11. doi: 10.1186/1471-2377-5-11. BMC Neurol. 2005. PMID: 15967032 Free PMC article.

8

Assessment of PINK1 (PARK6) polymorphisms in Finnish PD.

Clarimón J, Eerola J, Hellström O, Peuralinna T, Tienari PJ, Singleton AB. Clarimón J, et al. Neurobiol Aging. 2006 Jun;27(6):906-7. doi: 10.1016/j.neurobiolaging.2005.03.028. Epub 2005 Jul 19. Neurobiol Aging. 2006. PMID: 16046032

9

Conflicting results regarding the semaphorin gene (SEMA5A) and the risk for Parkinson disease.

Clarimon J, Scholz S, Fung HC, Hardy J, Eerola J, Hellstrom O, Chen CM, Wu YR, Tienari PJ, Singleton A. Clarimon J, et al. Am J Hum Genet. 2006 Jun;78(6):1082-4; author reply 1092-4. doi: 10.1086/504727. Am J Hum Genet. 2006. PMID: 16685660 Free PMC article. No abstract available.

10

Assessing the role of DRD5 and DYT1 in two different case-control series with primary blepharospasm.

Clarimon J, Brancati F, Peckham E, Valente EM, Dallapiccola B, Abruzzese G, Girlanda P, Defazio G, Berardelli A, Hallett M, Singleton AB. Clarimon J, et al. Mov Disord. 2007 Jan 15;22(2):162-6. doi: 10.1002/mds.21182. Mov Disord. 2007. PMID: 17133500

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